United States · FDA National Drug Code directory
DEFERASIROX
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 31722-031_17f07dc1-8041-d263-e063-6394a90ae223
- Product NDC
- 31722-031
- Form
- GRANULE
- Composition / generic term
- DEFERASIROX
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220922
- Source listing expiry
- 20261231
Source-listed ingredients
- DEFERASIROX — 360 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 PACKET in 1 CARTON (31722-031-32) / 1 GRANULE in 1 PACKET · 31722-031-32
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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